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  <title>Recall Radar latest recalls</title>
  <subtitle>Recent FDA food, drug, supplement, and medical device recalls from public openFDA enforcement data.</subtitle>
  <link href="https://notyetneeded.com/latest-recalls" rel="alternate" type="text/html"/>
  <link href="https://notyetneeded.com/atom.xml" rel="self" type="application/atom+xml"/>
  <updated>2026-09-24T00:30:29.452Z</updated>
  <author>
    <name>Not Yet Needed</name>
  </author>
  <entry>
    <id>https://notyetneeded.com/recalls/Drugs-99837-20260916</id>
    <title>Drugs: fentaNYL Citrate, 1,000 mcg/100 mL (10mcg/mL) Injection solution in 100 mL, 0.9% NaCl Bag, OurPharma LLC, 2512 S. City L...</title>
    <link href="https://api.fda.gov/drug/enforcement.json?search=event_id%3A%2299837%22" rel="alternate"/>
    <updated>2026-09-16T00:00:00.000Z</updated>
    <summary>Not Yet Classified | Ongoing | Firm: OurPharma LLC | Reason: Labeling: Not Elsewhere Classified: Complaint received on 08/31/2026 regarding the discrepancy of the IV bag expiry (07/31/2026 and 11/30/2026) and the product expiry (12/09/2026). | Distribution: Nationwide within the U.S | Recall began: 2026-09-03 | FDA IDs: / event 99837</summary>
  </entry>
  <entry>
    <id>https://notyetneeded.com/recalls/D-0836-2026</id>
    <title>Drugs: Fluphenazine Hydrochloride Tablets, USP, 1mg, 100-count bottles, Rx Only, Marketed by: Ajanta Pharma USA Inc., Bridgewat...</title>
    <link href="https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0836-2026%22" rel="alternate"/>
    <updated>2026-09-16T00:00:00.000Z</updated>
    <summary>Class III | Ongoing | Firm: Ajanta Pharma USA Inc | Reason: Failed impurities/degradation specifications: (OOS) for Organic Impurities by HPLC (Impurity-A) during testing at the 18 months long term stability. Result: 1.1 percent. Spec: 1.0 percent. | Distribution: Nationwide within the U.S | Recall began: 2026-08-25 | FDA IDs: D-0836-2026 / event 99733</summary>
  </entry>
  <entry>
    <id>https://notyetneeded.com/recalls/D-0835-2026</id>
    <title>Drugs: Povidone Iodine 1.25% / Proparacaine HCl 0.5% Ophthalmic Solution, 10 mL per dropper bottle, For Office Use Only, Imprim...</title>
    <link href="https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0835-2026%22" rel="alternate"/>
    <updated>2026-09-16T00:00:00.000Z</updated>
    <summary>Class III | Ongoing | Firm: ImprimisRx NJ LLC | Reason: Subpotent Drug | Distribution: USA Nationwide | Recall began: 2026-08-24 | FDA IDs: D-0835-2026 / event 99756</summary>
  </entry>
  <entry>
    <id>https://notyetneeded.com/recalls/H-1341-2026</id>
    <title>Food: Alfalfa, Net Weight 50 lbs. bag, Product of USA, International Specialty Supply 1011 Volunteer Dr. Cookeville, TN 38506</title>
    <link href="https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1341-2026%22" rel="alternate"/>
    <updated>2026-09-16T00:00:00.000Z</updated>
    <summary>Class I | Ongoing | Firm: International Sprout Holdings, Inc | Reason: Potential E. coli and Salmonella contamination | Distribution: Wholesale consignees in 16 states: CA, FL, HI, IL, MA, MN, MO, MT, NY, OH, OR, PA, TN, SC, TX, UT; Puerto Rico; Canada, Mexico, Tahiti, and Venezuela | Recall began: 2026-08-23 | FDA IDs: H-1341-2026 / event 99822</summary>
  </entry>
  <entry>
    <id>https://notyetneeded.com/recalls/D-0850-2026</id>
    <title>Drugs: Dextrose Injection, USP, 70 %, 2000 mL bags, Rx Only, Baxter Healthcare Corporation Deerfield, IL, 60016, Made in USA, N...</title>
    <link href="https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0850-2026%22" rel="alternate"/>
    <updated>2026-09-16T00:00:00.000Z</updated>
    <summary>Class I | Ongoing | Firm: Baxter Healthcare Corporation | Reason: Presence of Particulate Matter: particulate matter identified as stainless steel particles in the solution. | Distribution: U.S. Nationwide. | Recall began: 2026-08-17 | FDA IDs: D-0850-2026 / event 99679</summary>
  </entry>
  <entry>
    <id>https://notyetneeded.com/recalls/H-1334-2026</id>
    <title>Food: Fannie May &amp; XO Marshmallow Pixie S&#39;mores Collection, 4.47oz</title>
    <link href="https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1334-2026%22" rel="alternate"/>
    <updated>2026-09-16T00:00:00.000Z</updated>
    <summary>Class II | Ongoing | Firm: Ferrero USA | Reason: Undeclared milk and pecans | Distribution: IA, IL, IN, OH | Recall began: 2026-08-14 | FDA IDs: H-1334-2026 / event 99682</summary>
  </entry>
  <entry>
    <id>https://notyetneeded.com/recalls/H-1330-2026</id>
    <title>Food: Momchipz Gluten Free Veggie Chips Broccoli Florets &amp; Cauliflower, net wt. 3oz (85g). UPC 6 28634 44216 6. Ingredients: B...</title>
    <link href="https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1330-2026%22" rel="alternate"/>
    <updated>2026-09-16T00:00:00.000Z</updated>
    <summary>Class I | Ongoing | Firm: EXOTIQUE FOODS CANADA | Reason: Undeclared Wheat. | Distribution: Product was sold in the U.S. | Recall began: 2026-08-07 | FDA IDs: H-1330-2026 / event 99636</summary>
  </entry>
  <entry>
    <id>https://notyetneeded.com/recalls/H-1335-2026</id>
    <title>Food: Prolon Everyday Apulian Almond &amp; Cocoa Spread, NET WT: 8.47 OZ. Product packaged in glass jar with white label and gold...</title>
    <link href="https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1335-2026%22" rel="alternate"/>
    <updated>2026-09-16T00:00:00.000Z</updated>
    <summary>Class II | Ongoing | Firm: L-Nutra Inc | Reason: Undeclared allergen (tree nuts): hazelnut, cashew, and pistachio. | Distribution: Product is sold exclusively from the recalling firm&#39;s online website nationwide. | Recall began: 2026-08-07 | FDA IDs: H-1335-2026 / event 99675</summary>
  </entry>
  <entry>
    <id>https://notyetneeded.com/recalls/Z-3111-2026</id>
    <title>Devices: Getinge PVC Thoracic Catheter, Soft PVC Straight, 10 per Case; Size(Model Number): 1. 16FR(8016), 2. 24FR(8024), 3. 28FR...</title>
    <link href="https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3111-2026%22" rel="alternate"/>
    <updated>2026-09-16T00:00:00.000Z</updated>
    <summary>Class II | Ongoing | Firm: Atrium Medical Corporation | Reason: An Out of Specification result (OOS) related to bacterial endotoxin testing in a single lot of catheters. | Distribution: US Nationwide distribution. | Recall began: 2026-08-07 | FDA IDs: Z-3111-2026 / event 99680</summary>
  </entry>
  <entry>
    <id>https://notyetneeded.com/recalls/Z-3113-2026</id>
    <title>Devices: Getinge PVC Thoracic Catheter, Firm PVC Straight, 10 per Case; Size(Model Number): 1. 28FR(15028), 2. 36FR(15036);</title>
    <link href="https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3113-2026%22" rel="alternate"/>
    <updated>2026-09-16T00:00:00.000Z</updated>
    <summary>Class II | Ongoing | Firm: Atrium Medical Corporation | Reason: An Out of Specification result (OOS) related to bacterial endotoxin testing in a single lot of catheters. | Distribution: US Nationwide distribution. | Recall began: 2026-08-07 | FDA IDs: Z-3113-2026 / event 99680</summary>
  </entry>
  <entry>
    <id>https://notyetneeded.com/recalls/Z-3110-2026</id>
    <title>Devices: Product Name: DermaV Laser System Model/Catalog Number: DermaV Medical laser device that delivers pulsed laser energy at...</title>
    <link href="https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3110-2026%22" rel="alternate"/>
    <updated>2026-09-16T00:00:00.000Z</updated>
    <summary>Class II | Ongoing | Firm: Lutronic Corporation | Reason: Utilizing higher fluences at 1064nm wavelength with current cryogen parameters may result in a spark/loud noise during treatment, potentially resulting in patient burn. | Distribution: Worldwide distribution - US Nationwide and the countries of Canada and European Union. | Recall began: 2026-08-06 | FDA IDs: Z-3110-2026 / event 99601</summary>
  </entry>
  <entry>
    <id>https://notyetneeded.com/recalls/Z-3133-2026</id>
    <title>Devices: MedicaLyte Liquid Bicarbonate Concentrate REF: BC-100 and BC+201</title>
    <link href="https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3133-2026%22" rel="alternate"/>
    <updated>2026-09-16T00:00:00.000Z</updated>
    <summary>Class II | Ongoing | Firm: Nipro Renal Soultions USA, Corporation | Reason: Hemodialysis concentrates contain high endotoxin levels | Distribution: Worldwide - US Nationwide distribution in the states of FL, GA, IL, MD, MI, NC, NJ, NV, OH, PA, and the countries of Guatemala and Panama. | Recall began: 2026-08-05 | FDA IDs: Z-3133-2026 / event 99573</summary>
  </entry>
  <entry>
    <id>https://notyetneeded.com/recalls/Z-3134-2026</id>
    <title>Devices: MedicaLyte Bicarbonate Powder REF: DB+201-2.1(45X) and DB+201-25 (35X, 36.83X, 45X))</title>
    <link href="https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3134-2026%22" rel="alternate"/>
    <updated>2026-09-16T00:00:00.000Z</updated>
    <summary>Class II | Ongoing | Firm: Nipro Renal Soultions USA, Corporation | Reason: Hemodialysis concentrates contain high endotoxin levels | Distribution: Worldwide - US Nationwide distribution in the states of FL, GA, IL, MD, MI, NC, NJ, NV, OH, PA, and the countries of Guatemala and Panama. | Recall began: 2026-08-05 | FDA IDs: Z-3134-2026 / event 99573</summary>
  </entry>
  <entry>
    <id>https://notyetneeded.com/recalls/Z-3136-2026</id>
    <title>Devices: Citric Complete Liquid Citric Acid Concentrate REF: LC+200-D,LC+201, LC+225(45X)</title>
    <link href="https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3136-2026%22" rel="alternate"/>
    <updated>2026-09-16T00:00:00.000Z</updated>
    <summary>Class II | Ongoing | Firm: Nipro Renal Soultions USA, Corporation | Reason: Hemodialysis concentrates contain high endotoxin levels | Distribution: Worldwide - US Nationwide distribution in the states of FL, GA, IL, MD, MI, NC, NJ, NV, OH, PA, and the countries of Guatemala and Panama. | Recall began: 2026-08-05 | FDA IDs: Z-3136-2026 / event 99573</summary>
  </entry>
  <entry>
    <id>https://notyetneeded.com/recalls/H-1331-2026</id>
    <title>Food: Crown Farms Dried Suri Cut, 200 gm, in plastic pack, 25 packages per box, keep frozen</title>
    <link href="https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1331-2026%22" rel="alternate"/>
    <updated>2026-09-16T00:00:00.000Z</updated>
    <summary>Class I | Ongoing | Firm: EURO FOODS GROUP USA NJ INC | Reason: The firm imported and distributed dried ribbon fish that was not properly eviscerated prior to drying. | Distribution: The adulterated product was distributed to the following states: VA, NY, NJ, MI | Recall began: 2026-08-01 | FDA IDs: H-1331-2026 / event 99684</summary>
  </entry>
  <entry>
    <id>https://notyetneeded.com/recalls/Z-3138-2026</id>
    <title>Devices: AMS Convenience Kit: DSAEK Pack - RX, Part Number AMS12394B</title>
    <link href="https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3138-2026%22" rel="alternate"/>
    <updated>2026-09-16T00:00:00.000Z</updated>
    <summary>Class II | Ongoing | Firm: Windstone Medical Packaging, Inc. | Reason: The convenience kits contain .0.9% Sodium Chloride Injection, USP products in Single Dose freeflex bags, which may contain blue Break-off-Parts (BOPs) that have detached from the infusion port during manipulation. | Distribution: US Nationwide distribution in the states of CA, GA, WA. | Recall began: 2026-07-29 | FDA IDs: Z-3138-2026 / event 99658</summary>
  </entry>
  <entry>
    <id>https://notyetneeded.com/recalls/Z-3120-2026</id>
    <title>Devices: HeartSine SAM 350P 350P US Device, US English - 2 Min CPR UDI-DI codes: 0506016712067 350P US Device, US English (Americ...</title>
    <link href="https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3120-2026%22" rel="alternate"/>
    <updated>2026-09-16T00:00:00.000Z</updated>
    <summary>Class II | Ongoing | Firm: HeartSine Technologies Ltd | Reason: Due to a damaged (over stretched) membrane tail that causes an intermittent fault. | Distribution: Worldwide - U.S. Nationwide distribution including in the states of AK, AL, AZ, CA, CT, DC, FL, GA, HI, IA, ID, IL, IN, KS, KY, MA, MD, ME MI, MN, NC, NJ, NM, NV, NY, OH, OK, OR, PA, SD,TN, TX, UT, VA, WA, WI, WV and WY. The countries of Argentina, Australia,... | Recall began: 2026-07-27 | FDA IDs: Z-3120-2026 / event 99568</summary>
  </entry>
  <entry>
    <id>https://notyetneeded.com/recalls/Z-3114-2026</id>
    <title>Devices: Products that contain the Pericare Wipes: Bardex Lubricath Foley Catheter Tray REF: 899914 899916 899918 UDI codes: 0080...</title>
    <link href="https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3114-2026%22" rel="alternate"/>
    <updated>2026-09-16T00:00:00.000Z</updated>
    <summary>Class II | Ongoing | Firm: C.R. Bard Inc | Reason: Due to complaints received indicating presence of contamination on the surface of pericare wipes provided with various Foley and Intermittent Catheter Trays. | Distribution: Worldwide - U.S. Nationwide distribution including in the states of AK, AL, AR, AZ, CA, CO, CT, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, WA, WI and W... | Recall began: 2026-06-25 | FDA IDs: Z-3114-2026 / event 98840</summary>
  </entry>
  <entry>
    <id>https://notyetneeded.com/recalls/Z-3115-2026</id>
    <title>Devices: Products that contain the Pericare Wipes: Bard¿ Foley Tray With Lubri-Sil¿ All-Silicone Foley Catheter REF: 947314 94731...</title>
    <link href="https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3115-2026%22" rel="alternate"/>
    <updated>2026-09-16T00:00:00.000Z</updated>
    <summary>Class II | Ongoing | Firm: C.R. Bard Inc | Reason: Due to complaints received indicating presence of contamination on the surface of pericare wipes provided with various Foley and Intermittent Catheter Trays. | Distribution: Worldwide - U.S. Nationwide distribution including in the states of AK, AL, AR, AZ, CA, CO, CT, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, WA, WI and W... | Recall began: 2026-06-25 | FDA IDs: Z-3115-2026 / event 98840</summary>
  </entry>
  <entry>
    <id>https://notyetneeded.com/recalls/Z-3118-2026</id>
    <title>Devices: Products that contain the Pericare Wipes: SureStep&quot; Foley Tray System Add-A-Foley Catheter REF: A153200 UDI code: 008017...</title>
    <link href="https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3118-2026%22" rel="alternate"/>
    <updated>2026-09-16T00:00:00.000Z</updated>
    <summary>Class II | Ongoing | Firm: C.R. Bard Inc | Reason: Due to complaints received indicating presence of contamination on the surface of pericare wipes provided with various Foley and Intermittent Catheter Trays. | Distribution: Worldwide - U.S. Nationwide distribution including in the states of AK, AL, AR, AZ, CA, CO, CT, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, WA, WI and W... | Recall began: 2026-06-25 | FDA IDs: Z-3118-2026 / event 98840</summary>
  </entry>
  <entry>
    <id>https://notyetneeded.com/recalls/Z-3119-2026</id>
    <title>Devices: Products that contain the Pericare Wipes: (Canada Only) SureStep&quot; Foley Tray System Bardex¿ IC Complete Care¿ REF: A3003...</title>
    <link href="https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3119-2026%22" rel="alternate"/>
    <updated>2026-09-16T00:00:00.000Z</updated>
    <summary>Class II | Ongoing | Firm: C.R. Bard Inc | Reason: Due to complaints received indicating presence of contamination on the surface of pericare wipes provided with various Foley and Intermittent Catheter Trays. | Distribution: Worldwide - U.S. Nationwide distribution including in the states of AK, AL, AR, AZ, CA, CO, CT, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, WA, WI and W... | Recall began: 2026-06-25 | FDA IDs: Z-3119-2026 / event 98840</summary>
  </entry>
  <entry>
    <id>https://notyetneeded.com/recalls/D-0833-2026</id>
    <title>Drugs: Trokendi XR, (topiramate) extended-release capsules, 50 mg, 30 Capsules, Rx only, Manufactured by: Catalent Pharma Solut...</title>
    <link href="https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0833-2026%22" rel="alternate"/>
    <updated>2026-09-09T00:00:00.000Z</updated>
    <summary>Class III | Ongoing | Firm: Supernus Pharmaceuticals, Inc. | Reason: Failed dissolution specifications. | Distribution: US Nationwide. | Recall began: 2026-08-31 | FDA IDs: D-0833-2026 / event 99767</summary>
  </entry>
  <entry>
    <id>https://notyetneeded.com/recalls/D-0834-2026</id>
    <title>Drugs: traZODone Hydrochloride Tablets, USP, 50 mg, Rx only, 100 Tablets, Manufactured in Croatia By: Pliva Hrvatska d.o.o, Zag...</title>
    <link href="https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0834-2026%22" rel="alternate"/>
    <updated>2026-09-09T00:00:00.000Z</updated>
    <summary>Class II | Ongoing | Firm: Teva Pharmaceuticals USA, Inc | Reason: Presence of Foreign Tablets/Capsules | Distribution: U.S. Nationwide | Recall began: 2026-08-24 | FDA IDs: D-0834-2026 / event 99734</summary>
  </entry>
  <entry>
    <id>https://notyetneeded.com/recalls/D-0840-2026</id>
    <title>Drugs: Buprenorphine Sublingual Tablets (C-III), 2 mg, 30 Tablets (3x10), Rx only, Distributed by: American Health Packaging, C...</title>
    <link href="https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0840-2026%22" rel="alternate"/>
    <updated>2026-09-09T00:00:00.000Z</updated>
    <summary>Class III | Ongoing | Firm: American Health Packaging | Reason: Labeling: Label Mix-up | Distribution: US Nationwide. | Recall began: 2026-08-19 | FDA IDs: D-0840-2026 / event 99674</summary>
  </entry>
  <entry>
    <id>https://notyetneeded.com/recalls/H-1304-2026</id>
    <title>Food: Prince ITALIAN BREAD; Sesame; NET WEIGHT 8 OZ. (227g); INGREDIENTS: ENRICHED BLEACHED FLOUR (WHEAT FLOUR, MALT BARLEY FL...</title>
    <link href="https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1304-2026%22" rel="alternate"/>
    <updated>2026-09-09T00:00:00.000Z</updated>
    <summary>Class III | Ongoing | Firm: Prince Bakery Inc | Reason: Sesame is not declared in the ingredient statement but is declared in the statement of identity. | Distribution: New York. | Recall began: 2026-08-13 | FDA IDs: H-1304-2026 / event 99646</summary>
  </entry>
  <entry>
    <id>https://notyetneeded.com/recalls/H-1305-2026</id>
    <title>Food: Prince ITALIAN BREAD; Sesame; ITALIAN &amp; FRENCH BREAD, LARGE; NET WEIGHT 12 OZ. (340g); INGREDIENTS: ENRICHED BLEACHED FL...</title>
    <link href="https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1305-2026%22" rel="alternate"/>
    <updated>2026-09-09T00:00:00.000Z</updated>
    <summary>Class III | Ongoing | Firm: Prince Bakery Inc | Reason: Sesame is not declared in the ingredient statement but is declared in the statement of identity. | Distribution: New York. | Recall began: 2026-08-13 | FDA IDs: H-1305-2026 / event 99646</summary>
  </entry>
  <entry>
    <id>https://notyetneeded.com/recalls/D-0811-2026</id>
    <title>Drugs: Vasopressin, in 0.9% Sodium Chloride Injection, 20 units per 100 mL (0.2 units/mL), 100mL Single-Dose Container, Rx only...</title>
    <link href="https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0811-2026%22" rel="alternate"/>
    <updated>2026-09-09T00:00:00.000Z</updated>
    <summary>Class II | Ongoing | Firm: Baxter Healthcare Corporation | Reason: CGMP Deviations | Distribution: US Nationwide; Puerto Rico; and Chile. | Recall began: 2026-08-06 | FDA IDs: D-0811-2026 / event 99500</summary>
  </entry>
  <entry>
    <id>https://notyetneeded.com/recalls/D-0813-2026</id>
    <title>Drugs: CARDENE IV (Nicardipine Hydrochloride) in 0.83% Sodium Chloride Injection, 40 mg in 200 mL (0.2 mg/mL) in GALAXY Single-...</title>
    <link href="https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0813-2026%22" rel="alternate"/>
    <updated>2026-09-09T00:00:00.000Z</updated>
    <summary>Class II | Ongoing | Firm: Baxter Healthcare Corporation | Reason: CGMP Deviations | Distribution: US Nationwide; Puerto Rico; and Chile. | Recall began: 2026-08-06 | FDA IDs: D-0813-2026 / event 99500</summary>
  </entry>
  <entry>
    <id>https://notyetneeded.com/recalls/D-0815-2026</id>
    <title>Drugs: Clindamycin Injection USP in 5% Dextrose, 900 mg per 50 mL (12 mg/mL) in GALAXY 50 mL Single Dose Container, Rx only, St...</title>
    <link href="https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0815-2026%22" rel="alternate"/>
    <updated>2026-09-09T00:00:00.000Z</updated>
    <summary>Class II | Ongoing | Firm: Baxter Healthcare Corporation | Reason: CGMP Deviations | Distribution: US Nationwide; Puerto Rico; and Chile. | Recall began: 2026-08-06 | FDA IDs: D-0815-2026 / event 99500</summary>
  </entry>
  <entry>
    <id>https://notyetneeded.com/recalls/D-0821-2026</id>
    <title>Drugs: Daptomycin, in 0.9% Sodium Chloride Injection, 1,000 mg per 100 mL (10 mg/mL), 1,000 mg total, in 1000 mL Single Dose Co...</title>
    <link href="https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0821-2026%22" rel="alternate"/>
    <updated>2026-09-09T00:00:00.000Z</updated>
    <summary>Class II | Ongoing | Firm: Baxter Healthcare Corporation | Reason: CGMP Deviations | Distribution: US Nationwide; Puerto Rico; and Chile. | Recall began: 2026-08-06 | FDA IDs: D-0821-2026 / event 99500</summary>
  </entry>
  <entry>
    <id>https://notyetneeded.com/recalls/H-1308-2026</id>
    <title>Food: Weis (Fresh From the Orchard ) Pasteurized Apple Cider, Contains 100 % Juice, the product comes in the following sizes:...</title>
    <link href="https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1308-2026%22" rel="alternate"/>
    <updated>2026-09-09T00:00:00.000Z</updated>
    <summary>Class II | Ongoing | Firm: WEIS MARKETS, INC. | Reason: Product has high patulin levels | Distribution: The recalled product was distributed to the State of PA. | Recall began: 2026-08-06 | FDA IDs: H-1308-2026 / event 99638</summary>
  </entry>
  <entry>
    <id>https://notyetneeded.com/recalls/D-0851-2026</id>
    <title>Drugs: Glutathione 200 mg/mL, 30 mL sterile multidose vial, Each vial contains: Glutathione, Ascorbic Acid, Benzyl Alcohol &amp; st...</title>
    <link href="https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0851-2026%22" rel="alternate"/>
    <updated>2026-09-09T00:00:00.000Z</updated>
    <summary>Class I | Ongoing | Firm: OPTIMAL BALANCE PHARMACY | Reason: Microbial Contamination of Sterile Products - out of specifications results were obtained for bacterial endotoxin. | Distribution: USA Nationwide. | Recall began: 2026-08-05 | FDA IDs: D-0851-2026 / event 99662</summary>
  </entry>
  <entry>
    <id>https://notyetneeded.com/recalls/H-1327-2026</id>
    <title>Food: Bread Pudding with Vanilla Sauce - KIT NET WT 4 LB (1.81Kg) UPC 7 22515 91732 0 Ukrop&#39;s Homestyle Foods, LLC Richmond, V...</title>
    <link href="https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1327-2026%22" rel="alternate"/>
    <updated>2026-09-09T00:00:00.000Z</updated>
    <summary>Class II | Ongoing | Firm: Ukrop&#39;s Homestyle Foods LLC | Reason: Foreign object: metal fragments | Distribution: Product was shipped to the following states: KY, NC, VA &amp; WVA. | Recall began: 2026-07-30 | FDA IDs: H-1327-2026 / event 99548</summary>
  </entry>
  <entry>
    <id>https://notyetneeded.com/recalls/H-1320-2026</id>
    <title>Food: Wonton Specialist Inc. Pan Fried Noodle, 16 oz and 5lb packaged in clear plastic bags</title>
    <link href="https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1320-2026%22" rel="alternate"/>
    <updated>2026-09-09T00:00:00.000Z</updated>
    <summary>Class III | Ongoing | Firm: Wonton Specialists | Reason: Undeclared FD&amp;C Red No. 40 | Distribution: NY, NJ, PA | Recall began: 2026-07-28 | FDA IDs: H-1320-2026 / event 99508</summary>
  </entry>
  <entry>
    <id>https://notyetneeded.com/recalls/H-1325-2026</id>
    <title>Food: Wonton Specialist Inc. Cooked Noodle, 16 oz and 5 lb - packaged in clear plastic bags</title>
    <link href="https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1325-2026%22" rel="alternate"/>
    <updated>2026-09-09T00:00:00.000Z</updated>
    <summary>Class III | Ongoing | Firm: Wonton Specialists | Reason: Undeclared FD&amp;C Red No. 40 | Distribution: NY, NJ, PA | Recall began: 2026-07-28 | FDA IDs: H-1325-2026 / event 99508</summary>
  </entry>
  <entry>
    <id>https://notyetneeded.com/recalls/H-1329-2026</id>
    <title>Food: OLA-OLA Pounded Yam (Iyan) IYANINSTANT, NET WT. 2 lbs., 4 lbs., 5 lbs., 10 lbs, packed in flexible plastic bags. INGREDI...</title>
    <link href="https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1329-2026%22" rel="alternate"/>
    <updated>2026-09-09T00:00:00.000Z</updated>
    <summary>Class I | Ongoing | Firm: Fayus Inc. | Reason: Undeclared milk. | Distribution: Domestic: CA, GA, IL, NJ, NY, TX Foreign: Canada, Australia | Recall began: 2026-07-06 | FDA IDs: H-1329-2026 / event 99368</summary>
  </entry>
</feed>
